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Q34629238-6F32B32E-84A2-4047-AF8C-0373B0D4B2C6
Q34629238-6F32B32E-84A2-4047-AF8C-0373B0D4B2C6
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Statement
http://www.wikidata.org/entity/statement/Q34629238-6F32B32E-84A2-4047-AF8C-0373B0D4B2C6
Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.
P2860
Q34629238-6F32B32E-84A2-4047-AF8C-0373B0D4B2C6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34629238-6F32B32E-84A2-4047-AF8C-0373B0D4B2C6
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wasDerivedFrom
fc215fd01f5536cd0ddf8ed6a6b1809039f12633
P2860
FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletions.